Results 111 to 120 of about 1,223,943 (215)

Atypical presentation of a hormonally active adrenocortical tumor in an adolescent leading to delayed diagnosis

open access: yes, 2011
Adrenocortical tumors are rare in children and present with variable signs depending on the type of hormone excess. We herein describe the unusual presentation of a child with adrenocortical tumor and introduce the concept of in vitro chemosensitivity ...
Mullis, Primus E   +5 more
core  

Estrogen-secreting adrenocortical tumor in a postmenopausal woman: a challenging diagnosis. [PDF]

open access: yesEndocrinol Diabetes Metab Case Rep, 2021
Mermejo LM   +8 more
europepmc   +1 more source

Combination of sorafenib and everolimus impacts therapeutically on adrenocortical tumor models.

open access: yes, 2012
Treatment options are insufficient in patients with adrenocortical carcinoma. Based on efficacy of sorafenib, a tyrosine kinase inhibitor, and everolimus, an inhibitor of the mammalian target of rapamycin (mTOR) in tumors of different histotype, we aimed
Cicala MV   +10 more
core   +1 more source

A case of infantile virilizing adrenocortical tumor [PDF]

open access: yes, 1989
The patient was a 16-month-old girl, born by mature natural delivery and weighing 3, 320 g. Hirsutism was noted on birth. Development of pubic hair and hypertrophy of the labia minora were noted after 8 months. At the time of admission, the height was 80
平尾, 佳彦   +10 more
core  

Case report: Ipilimumab and nivolumab in metastatic adrenocortical cancer with high tumor mutational burden

open access: yesFrontiers in Oncology
In the setting of metastatic adrenocortical cancer, there are limited therapy options such as mitotane and platinum-based chemotherapy with only low response rates. Ipilimumab and nivolumab are approved for several solid cancer types.
Rebekka Mispelbaum   +5 more
doaj   +1 more source

Carcinoma adreno-cortical: análise de 29 casos [PDF]

open access: yes, 2005
Trabalho de Conclusão de Curso - Universidade Federal de Santa Catarina. Curso de Medicina.
Silva, Ricardo Kupka da
core  

molecular clinical case Clinical and molecular aspects of a pediatric metachronous adrenocortical tumor Aspectos clínicos e moleculares de tumor adrenocortical metacrônico pediátrico

open access: yes, 2011
SUMMARY The occurrence of metachronous adrenocortical carcinoma has rarely been described. We report a case of a child with virilizing adrenocortical metachronous tumors that, despite several metastases, presented long-term survival (15 years).
Oliveira Lima   +11 more
core  

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